Known databases for pathogenic SNV's in the non coding regions

Question

[osiemen]

Is there any database available for known pathogenic non coding SNV's ?

I want to use it for validation.

All tips are welcome!

Answer 1

[Pierre Lindenbaum]

A rough exploration using NCBI Clinvar and my tool xsltstream: http://lindenb.github.io/jvarkit/XsltStream.html

[osiemen]

thanks a lot dear Pierre!

[osiemen]

is there any chance to get the output in a Bed file format, i am interested in the positions of the mutations